FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756914956 · Model: 35-401067 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DeRoyal
Primary DI
00749756914956
Version / Model
35-401067
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-29
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a4f1f06e-93ec-458e-933f-da871b2a8a02

Device Description

MEDLINE MNFL W/20" EXT DUAL CHK VLV W/60" TBG

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXT INJECTOR AND SYRINGE, ANGIOGRAPHIC

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 50749756914951
Primary 00749756914956

Customer Contacts